- University of Rochester (Rochester, NY)
- …Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400081 General Pediatrics Work Shift: UR - Day (United States of America) Range: UR URG 106 H ... brings consistency, empathy, and technical expertise across all phases of study implementation, from participant recruitment and engagement through in-person and… more
- University of Michigan (Ann Arbor, MI)
- …respond accordingly + Possess critical thinking skills + Ability to triage complex study concerns appropriately ** Work Schedule** This is a full-time regular ... We are seeking a responsible, motivated, individual who will independently provide study coordination for simple and moderately complex clinical research studies… more
- University of Washington (Seattle, WA)
- …. Work with Regulatory Coordinator to develop and implement study tools and source documents, maintain regulatory documents, and review and complete ... Trials Unit supports a diverse portfolio of clinical research studies with a broad reach of diseases and patient...sponsors, IRB's and other regulatory authorities when applicable. . Work with monitors and sponsors to facility study… more
- University of Colorado (Aurora, CO)
- …+ Assist with and oversee the day-to-day operations of clinical trials and studies + Obtain study subject's medical history and current medication information, ... to protocols, informed consent forms, and all other essential study documents for assigned studies + Independently...duties **This position will require occasional after-hours and weekend work .** ** Work Location:** Hybrid **Why Join Us:**… more
- ConvaTec (Lexington, MA)
- …policies and SOPs. **Key Responsibilities:** + Working closely with Clinical Study Managers (CSMs) and Clinical Research Associates (CRAs), manage all operational ... aspects from start-up to close-out activities of studies to assure adherence to timelines, budget and milestones...closely with the Global Head of Clinical Operations, develop study level operational strategy and clinical operations plans in… more
- University of Southern California (Los Angeles, CA)
- … study sponsor. + Assists in participant recruitment for studies including recruitment, screening, orientation and correspondence. Schedules subject appointments, ... a lead coordinating aspects of sponsor-initiated and investigator-initiated research studies and D&I program including subject recruitment, data collection,… more
- Gilead Sciences, Inc. (Foster City, CA)
- …of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave ... of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave… more
- University of Colorado (Aurora, CO)
- …additional: + Clinical Research & Participant Engagement + Serve as primary study coordinator for multi-site studies , including oversight of site onboarding, ... + Clinical Research & Participant Engagement + Obtain consent/assent and conduct study visits with infants, children, and adults according to protocol, including… more
- IQVIA (Durham, NC)
- …and accelerate evidence generation to improve patient outcomes. In this role, you'll work closely with one sponsor, gaining deep knowledge of their therapies while ... leveraging IQVIA's global expertise. **Overview:** Design and conduct epidemiological studies to generate real-world evidence within time, budget, and quality… more
- University of Miami (Coral Gables, FL)
- …social support) on child health and development. The Research Associate I will work closely with the Miami-ECHO study leadership to recruit, enroll, and ... work with the ECHO Program, the candidate may work on other studies at the School...study sites - School of Nursing and Health Studies , Miller School of Medicine, collaborating Miami-Dade County organizations,… more